Time-domain separation of optical properties from structural transitions in resonantly bonded materials

Femtosecond optical spectroscopy and single-shot electron diffraction measurements during the photoinduced amorphization of the phase-change material Ge 2 Sb 2 Te 5 demonstrate that optical properties can be separated from the structural state. The extreme electro-optical contrast between crystallin...

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Veröffentlicht in:Nature materials 2015-10, Vol.14 (10), p.991-995
Hauptverfasser: Waldecker, Lutz, Miller, Timothy A., Rudé, Miquel, Bertoni, Roman, Osmond, Johann, Pruneri, Valerio, Simpson, Robert E., Ernstorfer, Ralph, Wall, Simon
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container_end_page 995
container_issue 10
container_start_page 991
container_title Nature materials
container_volume 14
creator Waldecker, Lutz
Miller, Timothy A.
Rudé, Miquel
Bertoni, Roman
Osmond, Johann
Pruneri, Valerio
Simpson, Robert E.
Ernstorfer, Ralph
Wall, Simon
description Femtosecond optical spectroscopy and single-shot electron diffraction measurements during the photoinduced amorphization of the phase-change material Ge 2 Sb 2 Te 5 demonstrate that optical properties can be separated from the structural state. The extreme electro-optical contrast between crystalline and amorphous states in phase-change materials is routinely exploited in optical data storage 1 and future applications include universal memories 2 , flexible displays 3 , reconfigurable optical circuits 4 , 5 , and logic devices 6 . Optical contrast is believed to arise owing to a change in crystallinity. Here we show that the connection between optical properties and structure can be broken. Using a combination of single-shot femtosecond electron diffraction and optical spectroscopy, we simultaneously follow the lattice dynamics and dielectric function in the phase-change material Ge 2 Sb 2 Te 5 during an irreversible state transformation. The dielectric function changes by 30% within 100 fs owing to a rapid depletion of electrons from resonantly bonded states. This occurs without perturbing the crystallinity of the lattice, which heats with a 2-ps time constant. The optical changes are an order of magnitude larger than those achievable with silicon and present new routes to manipulate light on an ultrafast timescale without structural changes.
doi_str_mv 10.1038/nmat4359
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subjects 639/301/1019/584
639/301/119/1002
639/301/119/995
639/766/1130
Amorphous materials
Biomaterials
Bonding
Condensed Matter Physics
Crystal lattices
Crystallinity
Data storage
Dielectrics
Lattices
letter
Logic
Materials Science
Nanotechnology
Optical and Electronic Materials
Optical properties
Phase transitions
Physics
Silicon
Spectroscopy
title Time-domain separation of optical properties from structural transitions in resonantly bonded materials
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